Holds one active US DMF and 3 valid CEPs for brimonidine, filing since 2007. Its 2023 FDA inspection closed as NAI, and its GMP is recognised in 16 markets.
Holds one active US DMF and 2 valid CEPs for brimonidine, filing since 2019. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 20 markets.
Holds one active US DMF and one valid CEP for brimonidine, filing since 2010. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 10 markets.
Holds one active US DMF and one valid CEP for brimonidine, filing since 2004. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 10 markets.
Holds 2 active US DMFs and one valid CEP for brimonidine, filing since 2008. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF and one valid CEP for brimonidine, filing since 2021. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Registered with SFDA (Saudi Arabia) for brimonidine. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
Open the full list with a free accountThis page filters the worldwide Brimonidine manufacturer list to companies based in India. The order is set by active filings weighted by regulator, inspection outcomes and their recency, breadth of GMP recognition, and evidence of real exports, less any open risk flags. Read the full method.
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